1x2t: Difference between revisions

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New page: left|200px<br /><applet load="1x2t" size="450" color="white" frame="true" align="right" spinBox="true" caption="1x2t, resolution 1.72Å" /> '''Crystal Structure of...
 
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[[Image:1x2t.gif|left|200px]]<br /><applet load="1x2t" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1x2t.gif|left|200px]]<br /><applet load="1x2t" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1x2t, resolution 1.72&Aring;" />
caption="1x2t, resolution 1.72&Aring;" />
'''Crystal Structure of Habu IX-bp at pH 6.5'''<br />
'''Crystal Structure of Habu IX-bp at pH 6.5'''<br />


==Overview==
==Overview==
Coagulation factor IX-binding protein, isolated from Trimeresurus, flavoviridis (IX-bp), is a C-type lectin-like protein. It is an, anticoagulant consisting of homologous subunits, A and B. Each subunit has, a Ca(2+)-binding site with a unique affinity (K(d) values of 14muM and, 130muM at pH 7.5). These binding characteristics are pH-dependent and, under acidic conditions, the Ca(2+) binding of the low-affinity site was, reduced considerably. In order to identify which site has high affinity, and to investigate the pH-dependent Ca(2+) release mechanism, we have, determined the crystal structures of IX-bp at pH 6.5 and pH 4.6 (apo, form), and compared the Ca(2+)-binding sites with each other and with, those of the solved structures under alkaline conditions; pH 7.8 and pH, 8.0 (complexed form). At pH 6.5, Glu43 in the Ca(2+)-binding site of, subunit A displayed two conformations. One (minor) is that in the alkaline, state, and the other (major) is that at pH 4.6. However, the corresponding, Gln43 residue of subunit B is in only a single conformation, which is, almost identical with that in the alkaline state. At pH 4.6, Glu43 of, subunit A adopts a conformation similar to that of the major conformer, observed at pH 6.5, while Gln43 of subunit B assumes a new conformation, and both Ca(2+) positions are occupied by water molecules. These results, showed that Glu43 of subunit A is much more sensitive to protonation than, Gln43 of subunit B, and the conformational change of Glu43 occurs around, pH6.5, which may correspond to the step of Ca(2+) release.
Coagulation factor IX-binding protein, isolated from Trimeresurus flavoviridis (IX-bp), is a C-type lectin-like protein. It is an anticoagulant consisting of homologous subunits, A and B. Each subunit has a Ca(2+)-binding site with a unique affinity (K(d) values of 14muM and 130muM at pH 7.5). These binding characteristics are pH-dependent and, under acidic conditions, the Ca(2+) binding of the low-affinity site was reduced considerably. In order to identify which site has high affinity and to investigate the pH-dependent Ca(2+) release mechanism, we have determined the crystal structures of IX-bp at pH 6.5 and pH 4.6 (apo form), and compared the Ca(2+)-binding sites with each other and with those of the solved structures under alkaline conditions; pH 7.8 and pH 8.0 (complexed form). At pH 6.5, Glu43 in the Ca(2+)-binding site of subunit A displayed two conformations. One (minor) is that in the alkaline state, and the other (major) is that at pH 4.6. However, the corresponding Gln43 residue of subunit B is in only a single conformation, which is almost identical with that in the alkaline state. At pH 4.6, Glu43 of subunit A adopts a conformation similar to that of the major conformer observed at pH 6.5, while Gln43 of subunit B assumes a new conformation, and both Ca(2+) positions are occupied by water molecules. These results showed that Glu43 of subunit A is much more sensitive to protonation than Gln43 of subunit B, and the conformational change of Glu43 occurs around pH6.5, which may correspond to the step of Ca(2+) release.


==About this Structure==
==About this Structure==
1X2T is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Trimeresurus_flavoviridis Trimeresurus flavoviridis] with CA and 1PE as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1X2T OCA].  
1X2T is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Trimeresurus_flavoviridis Trimeresurus flavoviridis] with <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=1PE:'>1PE</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1X2T OCA].  


==Reference==
==Reference==
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[[Category: heterodimer]]
[[Category: heterodimer]]


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